Maria Anvret

Characterization of the frequency of delta F508 mutation and CF haplotypes in Swedish families

M. Starborg, M. Anvret, M. Nordenskjöld, 1991, Clinical genetics.

Genetic linkage of Welander distal myopathy to chromosome 2p13

L. Edström, K. Borg, M. Anvret, 1999, Annals of neurology.

DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease

M. Hayden, M. Anvret, S. Andrew, 1993, Clinical genetics.

Low frequency of RET mutations in Hirschsprung disease in Sweden

C. Eng, M. Anvret, A. Nordenskjöld, 1998, Clinical genetics.